BeNeLux Regulatory
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Kintiga is seeking a Regulatory Affairs professional to lead BeNeLux regulatory activities, RIP, and local pharmacovigilance with QPPV responsibilities. The role spans regulatory, medical information, and market access tasks across BeNeLux with a strong emphasis on stakeholder engagement.
The position offers hybrid work with only one day per week in Ghent (Tuesday) and requires fluency in Dutch, French and English. A Master’s/PhD in science and prior pharma/consulting experience are essential.